Canonical Allele Identifier: PA2826210778
Gene: SLC1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1916692
ClinVar RCV Id: RCV002590619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182657.1:p.Val556Ile
CA5946994
NM_001195728.3:c.1666G>A